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Ghana medical device government fees

Row-level verified

FDA Ghana current fee schedule, reviewed for 2026, in USD.

14 fee lines100% exact amountscurrency USDFX rates 2026-08-26reviewed 2026-08-25
Fee lineOfficial amountUSD equivalentFrequencyProvenance
Imported product registration - Class I (low risk)
Payable in cedi equivalent.
USD 60$60.00Per product, per annumVerified
Imported product registration - Class II (medium risk)USD 100$100Per product, per annumVerified
Imported product registration - Class III/IV (high risk)USD 160$160Per product, per annumVerified
Locally manufactured product registrationGH¢ 250$22.36Per product, per annumVerified
Major variation - foreign productsUSD 500$500Per variationVerified
Minor variation - foreign productsUSD 300$300Per variationVerified
Major variation - local productsGH¢ 200$17.89Per variationVerified
Minor variation - local productsGH¢ 100$8.94Per variationVerified
Foreign GMP audit
USD 4,000 for sites in Africa; USD 7,500 outside Africa.
USD 4,000–7,500$4,000–$7,500Per auditVerified
Local facility inspection
Tiered by facility size (GH¢ 400/200/100/50); free-zone facilities pay GH¢ 5,000.
GH¢ 50–400$4.47–$35.77Per inspectionVerified
Storage-facility inspectionGH¢ 120–800$10.73–$71.54Per inspectionVerified
IVD laboratory analysisGH¢ 2,500$224Per analysisVerified
Equipment verification
Re-analysis after failure: GH¢ 150 per sample.
GH¢ 2,000$179Per verificationVerified
Advertisement approval
Fast-track: GH¢ 1,800; airing an unapproved advertisement: GH¢ 25,000.
GH¢ 600$53.66Per script, language and mediumVerified
Government fees only — service and testing costs are separate
  • Verification of imported registered equipment is charged at 1.30% of CIF value (formula, not tabulated as an exact row).
  • Imported registration fees are quoted in USD but collected in cedi equivalent.
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Exact amounts verified against the FDA Ghana fee schedule · full review 2026-08-25 · row IDs are stable — cite as government-fees:ghana:imported-registration-class-i